Evidence map›Paper›PMID 29976746›Full record

Trial reportHaematologica2018

Addition of the mammalian target of rapamycin inhibitor, everolimus, to consolidation therapy in acute myeloid leukemia: experience from the UK NCRI AML17 trial.

Alan K Burnett, Emma Das Gupta, Steve Knapper, Asim Khwaja, Marion Sweeney, Lars Kjeldsen, Timothy Hawkins, Sophie E Betteridge, Paul Cahalin, Richard E Clark and 3 more

Open access · goldAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Haematologica, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Defining the Optimal Total Number of Chemotherapy Courses in Younger Patients With Acute Myeloid Leukemia: A Comparison of Three Versus Four Courses.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2021
    Trial
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Targeting regulated cell death pathways in acute myeloid leukemia.Cancer drug resistance (Alhambra, Calif.) · 2023
    Review
  8. The dual role of autophagy in acute myeloid leukemia.Journal of hematology & oncology · 2022
    Review
  9. Review
  10. Review
  11. Endothelial mTOR maintains hematopoiesis during aging.The Journal of experimental medicine · 2020
    Article
  12. Review
  13. Review
  14. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 8 institutions in 3 countries.

Alan K BurnettFormerly Department of Haematology, Cardiff University School of Medicine, UK akburnett719@gmail.com.
Emma Das GuptaDepartment of Haematology, Nottingham University Hospital NHS Trust, UK.
Steve KnapperDepartment of Haematology, University Hospital of Wales, Cardiff, UK.
Asim KhwajaUniversity College, London Cancer Institute, UK.
Marion SweeneyDepartment of Haematology, University Hospital of Wales, Cardiff, UK.
Lars KjeldsenDepartment of Haematology, Rigshospitalet, Copenhagen, Denmark.
Timothy HawkinsDepartment of Haematology, Auckland City Hospital, New Zealand.
Sophie E BetteridgeCentre for Trials Research, Cardiff University School of Medicine, UK.
Paul CahalinDepartment of Haematology, Blackpool Victoria Hospital, UK.
Richard E ClarkDepartment of Haematology, Royal Liverpool University Hospital, UK.
Robert K HillsDepartment of Haematology, Royal Liverpool University Hospital, UK.
Nigel H RussellDepartment of Haematology, Nottingham University Hospital NHS Trust, UK.
UK NCRI AML Study Group
Cardiff University · GBNottingham University Hospitals NHS Trust · GBRoyal Liverpool University Hospital · GBUniversity Hospital of Wales · GBAuckland City Hospital · NZBlackpool Victoria Hospital · GBLondon Cancer · GBRigshospitalet · DK

Funding

Cancer Research UK 15954Cancer Research UK 25350
6 · The paper itself

Abstract

As part of the UK NCRI AML17 trial, adult patients with acute myeloid leukemia in remission could be randomized to receive the mammalian target of rapamycin inhibitor everolimus, sequentially with post-induction chemotherapy. Three hundred and thirty-nine patients were randomised (2:1) to receive everolimus or not for a maximum of 84 days between chemotherapy courses. The primary endpoint was relapse-free survival. At 5 years there was no difference in relapse-free survival [29%

Indexed as

Consolidation ChemotherapyLeukemia, Myeloid, AcuteAdolescentAdultAgedDisease-Free SurvivalEverolimusFemaleHumansMaleMiddle AgedSurvival RateTOR Serine-Threonine KinasesEverolimusMTOR protein, humanTOR Serine-Threonine Kinases

Identifiers

PMID29976746
PMCPMC6165825
OpenAlexW2823851424

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.